The kidney-specific proteome
The main function of the kidney is to maintain body homeostasis; regulate blood composition of water, electrolytes, solutes, buffers as well as the elimination of several organic compounds such as drugs and exogenous compounds. The kidney consists of different cell types organized into sub-anatomical tissue structures with distinct functions in different segments of the nephron. Transcriptome analysis shows that 72% (n=14387) of all human proteins (n=20090) are expressed in the kidney and 452 of these genes show an elevated expression in the kidney compared to other tissue types.
The kidney transcriptome
Transcriptome analysis of the kidney can be visualized with regard to the specificity and distribution of transcribed mRNA molecules (Figure 1). Specificity illustrates the number of genes with elevated or non-elevated expression in the kidney compared to other tissues. Elevated expression includes three subcategory types of elevated expression:
Distribution, on the other hand, visualizes how many genes have, or do not have, detectable levels (nTPM≥1) of transcribed mRNA molecules in the kidney compared to other tissues. As evident in Table 1, all genes elevated in kidney are categorized as:
Figure 1. (A) The distribution of all genes across the five categories based on transcript specificity in kidney as well as in all other tissues. (B) The distribution of all genes across the six categories, based on transcript detection (nTPM≥1) in kidney as well as in all other tissues.
As shown in Figure 1, 452 genes show some level of elevated expression in the kidney compared to other tissues. The three categories of genes with elevated expression in kidney compared to other organs are shown in Table 1. In Table 2, the 12 genes with the highest enrichment in kidney are defined.
Table 1. The number of genes in the subdivided categories of elevated expression in kidney.
Protein expression of genes elevated in kidney
In-depth analysis of the elevated genes in kidney using antibody-based protein profiling allowed us to visualize the expression patterns of these proteins in different functional compartments including glomeruli, proximal tubules, distal tubules and collecting ducts.
Proteins specifically expressed in glomerulus
The process of urine formation begins in the glomerulus, where an ultrafiltrate of plasma is formed, and the filtered fluid enters the renal tubules. The filter consists of three layers; the fenestrated endothelium, the basement membrane, and the podocyte slit diaphragm. The analysis of the glomerulus elevated proteins is well in line with the function of the glomerulus as a filtration apparatus assembling a slit diaphragm. The list of kidney elevated proteins includes several well-known glomeruli-associated genes, such as podocin (NPHS2) and nephrin (NPHS1), well established as proteins creating the filtration diaphragm making up a filter for large molecules.
Proteins specifically expressed in proximal tubule
Approximately 60% of the filtered Na+, Cl-, K+, Ca2+, H2O and more than 90% of the filtered HCO3- are absorbed along the proximal tubule. This is also the segment that normally reabsorbs virtually all the filtered glucose and amino acids. An additional function is the secretion of numerous organic anions and cations. Most of the proteins elevated in the kidney are localized to the proximal tubule, which is in line with the function of the proximal tubule as a compartment for reabsorption of small molecules back to the blood. This includes many genes coding for transport proteins responsible for specific adsorption of various small molecules. In particular, there are numerous members of the solute carrier family proteins (SLC) each binding specific small molecules. It is also reassuring to find several enzymes involved in the digestion of proteins, such as peptidases, to allow adsorption of amino acids and peptides originating from proteins transported into the proximal tubule. Examples of genes expressed in the proximal tubule are SLC22A8, localized in the basolateral surface (blood), and SLC22A13, localized in the luminal surface (urine). AGMAT, BHMT, DPYS, GGT1, RIDA, LRP2, PKLR and XPNPEP2 are all kidney elevated genes expressed in the proximal tubule.
Proteins specifically expressed in distal tubule
Both the distal tubule and collecting duct are the sites where critical regulatory hormones such as aldosterone and vasopressin regulate acid and potassium excretion and determine the final urinary concentration of K+, Na+, and Cl-. The distal tubule contains the most abundant and most tissue-specific protein in the kidney; (UMOD), although the specific function of this protein is yet somewhat unclear. Similarly, the well-known calbindin (CALB1) is also elevated in the distal tubules. In addition, the list of kidney elevated genes contains several receptors for electrolyte transport, including potassium, sodium, and calcium transporters, such as SLC12A1. Again this is in line with the function of the distal tubule being responsible for the reabsorption of electrolytes to the blood and excretion of potassium to the urine. Another example of a gene expressed in the distal tubule is SLC12A3.
Proteins specifically expressed in collecting duct
There are two different cell types in the collecting duct: principal cells and intercalated cells. Principal cells are the main site of salt and water transport, and intercalated cells are the key site for acid-base regulation. Examples of the genes expressed in the collecting duct are the aquaporin 2 (AQP2), localized in the luminal surface, and ATP6V0D2 localized only in the intercalated cells. TMEM213 is also a kidney elevated gene expressed in the collecting ducts.
Gene expression shared between kidney and other tissues
There are 139 group enriched genes expressed in kidney. Group enriched genes are defined as genes showing a 4-fold higher average level of mRNA expression in a group of 2-5 tissues, including kidney, compared to all other tissues.
To illustrate the relation of kidney tissue to other tissue types, a network plot was generated, displaying the number of genes with a shared expression between different tissue types.
Figure 2. An interactive network plot of the kidney enriched and group enriched genes connected to their respective enriched tissues (grey circles). Red nodes represent the number of kidney enriched genes and orange nodes represent the number of genes that are group enriched. The sizes of the red and orange nodes are related to the number of genes displayed within the node. Each node is clickable and results in a list of all enriched genes connected to the highlighted edges. The network is limited to group enriched genes in combinations of up to 4 tissues, but the resulting lists show the complete set of group enriched genes in the particular tissue.
The network plot shows that kidney shares most group enriched gene expression with the liver. One example of a protein expressed in both kidney and liver is BHMT2, an amino acid that plays a crucial role in methylation reactions. BHMT2 is expressed in hepatocytes in the liver and proximal tubules in the kidney.
The kidney is a specialized tissue that plays a vital role in maintaining body homeostasis. The main functions can be categorized as follows:
The kidneys form the first part of the urinary system and their principal function is to maintain homeostasis by the regulation of electrolytes and the acid-base balance. Kidney function is vital for regulating blood pressure and the kidneys are also a source for several important hormones such as erythropoietin, which regulates the production of red blood cells. Histologically, the renal parenchyma consists of four parts: glomeruli, tubules, interstitium and blood vessels. Glomeruli are complex vascular structures composed of specialized endothelial, epithelial and mesangial cells arranged around a basement membrane. The glomerulus arises from the afferent arteriole to form lobules then rejoin the vascular pole to drain into the efferent arteriole. Normally the lobules are poorly defined but highlighted in some disease processes. The capillaries lie within the lumen of the expanded proximal end of the nephron, or Bowman's space, which is lined on its parietal aspect by a layer of attenuated epithelial cells overlying a thick basement membrane. Together the epithelial cells and basement membrane comprise the Bowman's capsule. The function of the glomerulus is the filtration of the blood that leads to the formation of urine.
A complex tubular system begins at the urinary pole (where urine is first formed in the Bowman's space) that extends to the renal papilla. The system comprises the proximal tubule, the loop of Henle, distal tubule and collecting duct. The proximal tubule consists of convoluted and straight portions, lined by tall columnar cells with abundant, acidophilic cytoplasm rich in structures for active fluid transport. The loop of Henle has thin descending and thick ascending portions lined by cuboidal and columnar cells. The distal tubule is narrower and shorter than the proximal tubule and lined by low cuboidal cells that do not display the deeply acidophilic, granular cytoplasm characteristic of the proximal tubule. Cuboidal cells with pale acidophilic cytoplasm and central nuclei line the collecting ducts.
The interstitium is more easily conceptualized as space rather than a structure; it is visualized only when abnormal. The interstitium contains specialized interstitial cells and connective tissue elements. The larger renal blood vessels are structurally similar to those in other body sites.
Here, the protein-coding genes expressed in kidney are described and characterized, together with examples of immunohistochemically stained tissue sections that visualize corresponding protein expression patterns of genes with elevated expression in kidney.
Transcript profiling was based on a combination of two transcriptomics datasets (HPA and GTEx), corresponding to a total of 14590 samples from 54 different human normal tissue types. The final consensus normalized expression (nTPM) value for each tissue type was used for the classification of all genes according to the tissue-specific expression into two different categories, based on specificity or distribution.
Relevant links and publications
Uhlén M et al., Tissue-based map of the human proteome. Science (2015)